Description
Antimitotic chemotherapeutic which inhibits via reversible high-affinity binding to microtubules [1]. Induces apoptosis in a variety of cancer cell lines [2] however, tumor cells can quickly develop resistance to docetaxel via several mechanisms [3,4]. Can act in synergy with a variety of other anticancer agents including kinase inhibitors [5,6].
References:
1) Fabbri et al. (2008), Mitotic catastrophe and apoptosis induced by docetaxel in hormone-refractory prostate cancer cells; J. Cell Physiol, 217 494
2) Dosso and Berthold (2008), Docetaxel in the management of prostate cancer: current standard of care and future directions ; Expert Opin. Pharmacother, 9 1969
3) Homma et al. (2008), RPN2 gene confers docetaxel resistance in breast cancer; Nat. Med., 14 939
4) Kars et al. (2008), Reversal of Multidrug Resistance by Synthetic and Natural Compounds in Drug-Resistant MCF-7 Cell Lines Chemotherapy, 54 194
5) Wallin et al. (2012), GDC-0941, A Novel Class I Selective PI3K Inhibitor, Enhances the Efficacy of Docetaxel in Human Breast Cancer Models by Increasing Cell Death In vitro and In Vivo; Clin Cancer Res., May 14: Epub ahead of print.
6) Heinemann et al. (2011), Synergistic effects of oncolytic reovirus and docetaxel chemotherapy in prostate cancer; BMC Cancer, 11 221
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For research use only. Not for diagnostic or clinical use.